Porous aluminum oxide

ABSTRACT

The invention relates to a substrate material, which is highly porous and which is provided with a mechanically stable, component-penetrating framework structure made of alpha-Al 2 O 3 , to methods for producing the substrate material, and to the use of the substrate material.

The invention relates to porous aluminum oxide, methods for producing same, and use thereof.

Porous aluminum oxide is often used as substrate material for filtration applications or as a substrate material for catalysts (catalyst support). In the use as a catalyst support, in particular as a substrate material for gas phase reactions of ethylene to produce ethylene oxide, a high-porosity Al₂O₃ ceramic is usually used. However, the requirement for the highest porosity possible conflicts with the desire for the most solid substrates possible, i.e., substrates with low abrasion. For gas phase reactions, in addition a certain specific surface (BET 0.5 to 1.3 m²/g) and the lowest possible diffusion resistance in penetrating the reactants are necessary. A multimodal (at least bimodal) pore distribution characteristic promotes the diffusion behavior. The chemical composition may vary according to the prior art; however, alpha-Al₂O₃ substrates have proven successful in practice. In addition, reference is made to accompanying elements which may adversely affect the selectivity, such as a high SiO₂ content.

In the production of porous framework structures, the required sintering process is usually not maintained until the compression, and instead is interrupted. An increase in the porosity is often achieved using organic additives having a placeholder function. Pore distributions are thus obtained which are directly related to the grain sizes of the raw materials used. Large pore channels are thus preferably produced using large grains (see US 2003/162655). However, the use of large grains results in small specific surfaces and low mechanical stability, provided that no appreciable secondary phase quantity is added. In addition, larger quantities of organic additives do not fundamentally alter this behavior, since the framework structure is composed of Al₂O₃.

The object of the present invention, therefore, is to provide a substrate material for filtration applications or for catalysts (catalyst support), for example, which does not have the disadvantages of the prior art. The object of the present invention in particular is to provide a substrate material for filtration applications or for catalysts (catalyst support), for example, having a framework structure with the highest possible mechanical stability.

According to the invention, this object is achieved by a substrate material having the characterizing features of the main claim. The substrate material according to the invention has the highest possible Al₂O₃ content. Preferred embodiments are characterized in the subclaims.

The substrate material according to the invention contains 90% to almost 100% by weight, preferably 92 to 98% by weight, particularly preferably above 98% by weight, of Al₂O₃, based on the sum of all inorganic components. According to the invention, all known Al₂O₃ phases are usable in principle. Preferably used according to the invention are alpha-Al₂O₃ as well as Al₂O₃ precursors, for example Al(OH)₃, AlOOH, or transition aluminas. The substrate material according to the invention may contain trace impurities, depending on the raw material. The substrate material according to the invention preferably contains less than less than 0.05% by weight of TiO₂, less than 0.2% by weight but greater than 0.02% by weight, in particular less than 0.1% by weight but greater than 0.02% by weight, of Na₂O, and/or less than 1% by weight, in particular less than 0.6% by weight, of SiO₂.

The substrate material according to the invention has a highly porous, mechanically stable, component-penetrating framework structure; this mechanically stable framework structure according to the invention which imparts mechanical strength to the substrate material is achieved according to the invention not by a large secondary phase quantity, but, rather, by a specialized sintering technique coupled with a particular raw material selection of the quantities and grain sizes to be used. These measures allow the highly porous, mechanically stable, component-penetrating framework structure intended according to the invention.

The selection of the aluminum oxides to be used and of the quantities and grain sizes of organic substances to be used is essential to the invention, since, in addition to slight shrinkage due to relatively coarse Al₂O₃ having grain sizes of 3 to 5 μm, fine-grained Al₂O₃ having grain sizes of 0.3 to 1 μm is also necessary for achieving the sintering and the mechanical stability, as well as for achieving a defined specific surface according to the invention.

Tests have shown that the use of Al₂O₃ precursors, for example Al(OH)₃, AlOOH, or transition aluminas, is particularly advantageous for the high mechanical stability required according to the invention.

According to the invention, the highly porous, mechanically stable, component-penetrating framework composed of alpha-Al₂O₃ is formed by the use of certain additives in the production of the substrate material according to the invention. The additives selected according to the invention which are responsible for the pore formation, referred to below as pore-forming agents, play a special role in this regard.

Pore-forming agents of the inorganic as well as the organic type having certain grain sizes are materials which are added to the starting mixture, and which after the sintering and firing are completely removed from the substrate and completely burned off, thus providing a controlled porosity in the substrate material according to the invention. Examples of materials which may be used as pore-forming agents include carbon-containing materials such as carbon powder and graphite, powdered plastics such as polyethylene, polystyrene, and polycarbonate, resin, starch, cellulose and materials based on cellulose, wood flours, and other plant materials such as ground nut shells, for example pecan, cashew, walnut, and hazelnut shells. In addition, certain binders based on carbon may be used as pore-forming agents. Preferred pore-forming agents are organic pore-forming agents in nonswellable form, in particular materials derived from cellulose, such as ground nut shells, preferably walnut shell flour.

According to the invention, coarse organic components, preferably walnut shell flour having a relative grain size of 10 to 20 μm maximum and/or having a relative grain size of 100 to 500 μm maximum, are preferred in the production. The highly porous, mechanically stable, cohesive, component-penetrating framework structure of the alpha-Al₂O₃ obtained according to the invention, similar to a secondary phase, is situated in the gaps in the additive component, thus forming a second component-penetrating framework.

For producing an extrudable starting mixture for the substrate material according to the invention, binders known per se are used according to the invention, for example celluloses, substituted celluloses such as methylcellulose, ethylcellulose, and carboxyethylcellulose, stearates such as organic stearates, for example methyl stearate or ethyl stearate, waxes, polyolefin oxides, and mixtures of such binders or similar substances. According to the invention, water-swellable organic binders are preferred.

For minimizing the friction forces in the production of the substrate material according to the invention, lubricants may be used, for example colloidal silicic acid dispersions, waxes, and/or refined mineral oils.

The starting components selected according to the invention are mixed to form an extrudable compound, and the extrudable compound is subsequently molded into, for example, cylinders, rings, or similar shapes using suitable cutting and drying processes. Ring-shaped geometries may have, for example, an external diameter of 6 to 9.5 mm, an internal diameter of 2 to 5 mm, and a length of 5 to 9.5 mm. The molded bodies thus obtained are then sintered in the temperature range between 1350° C. and 1550° C. with residence times of 1 h to 10 h, preferably at temperatures of 1480° C. and with a residence time of 2 h.

The substrate material according to the invention thus obtained is highly porous and is provided with a mechanically stable, component-penetrating framework structure composed of alpha-Al₂O₃, and achieves the object of the invention.

The substrate material according to the invention preferably contains up to 30 to 90% by weight (based on the sum of all inorganic components) of a first alpha-Al₂O₃ component having a primary crystal grain size of 1 to 3 μm and an agglomerate size of 3 to 5 μm, and up to 10 to 70% by weight (based on the sum of all inorganic components) of a second alpha-Al₂O₃ component having a primary crystal grain size of 0.3 to 1 μm and an agglomerate size of 0.5 to 1 μm.

In another preferred embodiment, the highly porous substrate material according to the invention which is provided with a mechanically stable, component-penetrating framework structure contains, in addition to the first and second alpha-Al₂O₃ component, up to 50% by weight (based on the sum of all inorganic components) of an Al₂O₃ component which has been formed in situ from an Al₂O₃ precursor material during the production, preferably from Al(OH)₃, AlOOH, or transition aluminas, particularly preferably from Al(OH)₃ having a grain size of 1.3 μm.

In another preferred embodiment, the highly porous substrate material according to the invention which is provided with a mechanically stable, component-penetrating framework structure has a multimodal pore structure with high porosity, and at the same time has high mechanical strength.

In another preferred embodiment, the highly porous substrate material according to the invention which is provided with a mechanically stable, component-penetrating framework structure has a specific surface (measured according to BET) of 0.5 to 1.3 m²/g, in particular a specific surface of 0.5 to 0.95 m²/g.

In another preferred embodiment of the highly porous substrate material according to the invention which is provided with a mechanically stable, component-penetrating framework structure, the weight loss, determined as a measure of the abrasion resistance according to ASTM D 4058-81, is 5 to 40%.

In another preferred embodiment, the highly porous substrate material according to the invention which is provided with a mechanically stable, component-penetrating framework structure may absorb water in quantities between 41% and 60% (measured according to ASTM C 373-56).

In another preferred embodiment, the highly porous substrate material according to the invention which is provided with a mechanically stable, component-penetrating framework structure has breaking forces of greater than 50 N (determined in the vertex pressure process).

In another preferred embodiment, the highly porous substrate material according to the invention which is provided with a mechanically stable, component-penetrating framework structure has a pore diameter distribution curve (measured by mercury intrusion porosimetry) which has a relative maximum between 0.3 and 1.3 μm and another relative maximum between 15 and 60 μm.

In another preferred embodiment, the highly porous substrate material according to the invention which is provided with a mechanically stable, component-penetrating framework structure has further pore diameter maxima in the range of 100 to 500 μm in addition to the relative maxima which are determinable by mercury intrusion porosimetry.

In another preferred embodiment, the highly porous substrate material according to the invention which is provided with a mechanically stable, component-penetrating framework structure has a TiO₂ content of less than 0.05% by weight.

In another preferred embodiment, the highly porous substrate material according to the invention which is provided with a mechanically stable, component-penetrating framework structure has an Na₂O content of less than 0.2% by weight but greater than 0.02% by weight, in particular less than 0.1% by weight but greater than 0.02% by weight.

In another preferred embodiment, the highly porous substrate material according to the invention which is provided with a mechanically stable, component-penetrating framework structure has an SiO₂ content of less than 1% by weight, in particular less than 0.6% by weight, of SiO₂.

The present invention further relates to a method for producing the substrate material according to the invention which is provided with a mechanically stable, component-penetrating framework structure, in which, based on the sum of all inorganic components, 90 to almost 100% by weight, preferably 92 to 98% by weight, particularly preferably greater than 98% by weight, of Al₂O₃, between 5% by weight and 60% by weight of organic pore-forming agents in nonswellable form, between 0.5% by weight and 3% by weight of water-swellable organic binders, between 0.5% by weight and 5% by weight of organic liquids for minimizing the friction forces, and between 10% by weight and 30% by weight of water are mixed to form an extrudable compound, the extrudable compound is subsequently molded into, for example, cylinders, rings, or similar shapes using suitable cutting and drying processes, and the molded bodies thus obtained are sintered in the temperature range between 1350° C. and 1550° C. with residence times of 1 h to 10 h, preferably at temperatures of 1480° C. and with a residence time of 2 h.

A method for producing the substrate material according to the invention which is provided with a mechanically stable, component-penetrating framework structure is particularly preferred in which alpha-Al₂O₃, Al₂O₃ precursors, for example Al(OH)₃, AlOOH, or transition aluminas, or mixtures of these Al₂O₃ components is/are used as Al₂O₃.

A method for producing the substrate material according to the invention which is provided with a mechanically stable, component-penetrating framework structure is also preferred in which one or more organic pore-forming agents having a relative grain size of 10 to 20 μm maximum and/or having a relative grain size of 100 to 500 μm maximum are used as organic pore-forming agents.

A method for producing the substrate material according to the invention which is provided with a mechanically stable, component-penetrating framework structure is also preferred in which the organic pore-forming agents are selected from starch, walnut shell flour, pecan shell flour, polystyrene, polyethylene, polycarbonate, cellulose, wood flour, or carbon.

A method for producing the substrate material according to the invention which is provided with a mechanically stable, component-penetrating framework structure is also preferred in which the extrudable compound is molded into ring-shaped geometries using suitable cutting and drying processes, the ring-shaped geometries having, for example, an external diameter of 6 to 9.5 mm, an internal diameter of 2 to 5 mm, and a length of 5 to 9.5 mm.

The present invention further relates to the use of the substrate material according to the invention which is provided with a mechanically stable, component-penetrating framework structure as a catalyst support, as a catalyst support for ethylene oxide synthesis, for filtration purposes, and/or for filtration purposes for solid/liquid separation.

The examples listed in Table 1 and identified by Ex 1 through Ex 5 are intended to explain the present invention in greater detail without limiting same. The examples listed in Table 2 and identified by Comp 1 through Comp 5 are not according to the invention, but, rather, are used for comparison.

TABLE 1 Raw material Ex 1 Ex 2 Ex 3 Ex 4 Ex 5 Raw material characteristic Al₂O₃ (1) 50 50 50 40 50 Al₂O₃, primary grain: 2 μm, agglomerate: 4 μm, BET: 1.2 m²/9 Al₂O₃ (2) 20 50 0 30 10 Al₂O₃, primary grain: 0.5 μm, agglomerate: 0.7 μm, BET: 7 m²/g Spray powder 0 0 0 0 0 Spray powder composed of Al₂O₃ (1) (80) + Al₂O₃ (2) (20) + cornstarch (33) Al(OH)₃ 30 0 50 30 40 Al(OH)₃, primary grain: 1.3 μm, BET 3.5 m²/g Al₂O₃ (3) 0 0 0 0 0 Al₂O₃, primary grain: 1.2 μm, agglomerate: 1.4 μm, BET 3.7 m²/g Al₂O₃ (4) 0 0 0 0 0 Al₂O₃, primary grain 2 μm, agglomerate: 80 μm, BET: 1 m²/g Cornstarch 0 0 0 0 0 Cornstarch, organic pore-forming agent, 15 μm particles Cellulose 0 0 0 0 0 Cellulose, organic pore-forming agent, 120 μm particles Walnut shell flour 1 37.5 56.2 25 37.5 37.8 Walnut shell flour, organic pore- forming agent, 300 μm particles Walnut shell flour 2 0 0 0 0 0 Walnut shell flour, organic pore- forming agent, 180 μm particles Wax 0 0 0 3.1 3.1 Diamide wax, 15 μm particles Cellulose 2 1.9 1.9 1.9 3.1 3.1 Swellable cellulose, binder SiO₂ dispersion 0.38 0.38 0.38 0.38 0.38 Colloidal silicic acid dispersion, 40% solids Lubricant 3.5 3.5 3.5 3.5 3.5 Refined mineral oils, lubricant Water 27.5 32.5 30 30 31 Firing temperature/t 1480° C./2 h 1440° C./2 h 1480° C./2 h 1480° C./2 h 1480° C./2 h Water absorption in 48 50 50 48 55 See: ASTM C 373-56 % Weight loss in % 22 25 21 18 24 According to ASTM D 4058-81, 30 minutes Breaking force in N 100 130 97 100 90 Vertex pressure process BET 0.9 0.7 0.9 0.9 1 DIN ISO 9277 d50 pores 1 in μm 0.8 1 1.3 1 1.2 By mercury intrusion porosimetry d50 pores 2 in μm 50 50 35 55 55 By mercury intrusion porosimetry

TABLE 2 Raw material Comp 1 Comp 2 Comp 3 Comp 4 Comp 5 Raw material characteristic Al₂O₃ (1) 0 0 80 80 0 Al₂O₃, primary grain: 2 μm, agglomerate: 4 μm, BET: 1.2 m²/g Al₂O₃ (2) 20 20 0 0 20 Al₂O₃, primary grain: 0.5 μm, agglomerate: 0.7 μm, BET: 7 m²/g Spray powder 0 0 0 0 80 Spray powder composed of Al₂O₃ (1) (80) + Al₂O₃ (2) (20) + cornstarch (33) Al(OH)₃ 0 0 0 20 0 Al(OH)₃, primary grain: 1.3 μm, BET 3.5 m²/g Al₂O₃ (3) 0 0 20 0 0 Al₂O₃, primary grain: 1.2 μm, agglomerate: 1.4 μm, BET 3.7 m²/g Al₂O₃ (4) 80 80 0 0 0 Al₂O₃, primary grain 2 μm, agglomerate: 80 μm, BET: 1 m²/g Cornstarch 12.5 0 12.5 12.5 7.5 Cornstarch, organic pore-forming agent, 15 μm particles Cellulose 18.8 12.5 12.5 12.5 7.5 Cellulose, organic pore-forming agent, 120 μm particles Walnut shell flour 1 0 0 0 0 0 Walnut shell flour, organic pore- forming agent, 300 μm particles Walnut shell flour 2 0 12.5 12.5 18.8 0 Walnut shell flour, organic pore- forming agent, 180 μm particles Wax 0 0 0 0 0 Diamide wax, 15 μm particles Cellulose 2 2.5 5 2.5 2.5 6.2 Swellable cellulose, binder SiO₂ dispersion 1.1 1.1 1.1 1.1 3.8 Colloidal silicic acid dispersion, 40% solids Lubricant 3.5 3.5 3.5 3.5 3.2 Refined mineral oils, lubricant Water 32.5 37.7 33.8 41.2 47 Firing temperature/t 1480° C./2 h 1440° C./2 h 1440° C./2 h 1440° C./2 h 1440° C./2 h Water absorption in 44 52 44 59 53 See: ASTM C 373-56 % Weight loss in % 90 100 25 42 70 According to ASTM D 4058-81, 30 minutes Breaking force in N 20 25 40 38 41 Vertex pressure process BET 0.65 0.65 0.7 0.8 0.6 DIN ISO 9277 d50 pores 1 in μm 1 0.6 1 By mercury intrusion porosimetry d50 pores 2 in μm 7 10 5 6 8 By mercury intrusion porosimetry 

1-19. (canceled)
 20. A substrate material comprising a mechanically stable, component-penetrating framework structure composed of alpha-Al₂O₃, wherein the substrate material is highly porous.
 21. The substrate material according to claim 20, wherein the alpha-Al₂O₃ comprises up to 30 to 90% by weight based on the sum of all inorganic components of a first alpha-Al₂O₃ component having a primary crystal grain size of 1 to 3 μm and an agglomerate size of 3 to 5 μm, and up to 10 to 70% by weight based on the sum of all inorganic components of a second alpha-Al₂O₃ component having a primary crystal grain size of 0.3 to 1 μm and an agglomerate size of 0.5 to 1 μm.
 22. The substrate material according to claim 20, wherein the alpha-Al₂O₃ comprises up to 50% by weight based on the sum of all inorganic components of an Al₂O₃ component which has been formed in situ from an Al₂O₃ precursor material during the production.
 23. The substrate material according to claim 22, wherein the Al₂O₃ precursor is selected from the group consisting of Al(OH)₃, AlOOH and a transition alumina.
 24. The substrate material according to claim 23, wherein the Al₂O₃ precursor is Al(OH)₃ having a grain size of 1.3 μm.
 25. The substrate material according to claim 20, wherein the substrate material has a multimodal pore structure with high porosity, and at the same time has high mechanical strength.
 26. The substrate material according to claim 20, wherein the substrate material has a specific surface measured according to the BET method of from 0.5 to 1.3 m²/g.
 27. The substrate material according to claim 26, wherein the specific surface is from 0.5 to 0.95 m²/g.
 28. The substrate material according to claim 20, wherein the weight loss, determined as a measure of the abrasion resistance according to ASTM D 4058-81, is 5 to 40%.
 29. The substrate material according to claim 20, wherein the substrate material may absorb water in quantities between 41% and 60% measured according to ASTM C 373-56.
 30. The substrate material according to claim 20, wherein the substrate material has breaking forces of greater than 50 N (determined in the vertex pressure process).
 31. The substrate material according to claim 20, wherein the pore diameter distribution curve thereof measured by mercury intrusion porosimetry has a relative maximum between 0.3 and 1.3 μm and another relative maximum between 15 and 60 μm.
 32. The substrate material according to claim 20, wherein the substrate material has further pore diameter maxima in the range of 100 to 500 μm in addition to the relative maxima which are determinable by mercury intrusion porosimetry.
 33. The substrate material according to claim 20, wherein the substrate material has a TiO₂ content of less than 0.05% by weight.
 34. The substrate material according to claim 20, wherein the substrate material has an Na₂O content of less than 0.2% by weight but greater than 0.02% by weight.
 35. The substrate material according to claim 20, wherein the substrate material has an SiO₂ content of less than 1% by weight.
 36. A method for producing the substrate material comprising a mechanically stable, component-penetrating framework structure composed of alpha-Al₂O₃, wherein the substrate material is highly porous, comprising mixing from 90 to almost 100% by weight Al₂O₃ together with between 5% by weight and 60% by weight of an organic pore-forming agent in nonswellable form, between 0.5% by weight and 3% by weight of a water-swellable organic binder, between 0.5% by weight and 5% by weight of an organic liquid for minimizing friction forces, and between 10% by weight and 30% by weight of water to form an extrudable compound, molding the extrudable compound to form a bolded body, and sintering the molded body at a temperature in the range between 1350° C. and 1550° C. for 1 hour to 10 hours.
 37. A method according to claim 36, wherein at least one Al₂O₃ precursor selected form the group consisting of Al(OH)₃, AlOOH and a transition aluminas is present as the Al₂O₃.
 38. A method according to claim 36, wherein the organic pore-forming agent has a relative grain size of 10 to 20 μm maximum or having a relative grain size of 100 to 500 μm maximum.
 39. A method according to claim 36, wherein the organic pore-forming agent is selected from the group consisting of starch, walnut shell flour, pecan shell flour, polystyrene, polyethylene, polycarbonate, cellulose, wood flour and carbon.
 40. A method according to claim 36, wherein the extrudable compound is molded into ring-shaped geometries using suitable cutting and drying processes, the ring-shaped geometries having an external diameter of 6 to 9.5 mm, an internal diameter of 2 to 5 mm, and a length of 5 to 9.5 mm.
 41. A catalyst support comprising the substrate material of claim
 20. 42. A filter comprising the substrate material of claim 20 for filtration purposes. 